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UnknownCase fatality rate and associated factors in patients with 22q11 microdeletion syndrome: a retrospective cohort study.
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S-EPMC4225234 | biostudies-literature
UnknownCommon Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome.
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S-EPMC9225465 | biostudies-literature
UnknownContribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia.
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S-EPMC9797780 | biostudies-literature
UnknownInternational registry of dermatological manifestations secondary to COVID-19 infection in 347 Hispanic patients from 25 countries.
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S-EPMC8239526 | biostudies-literature
UnknownImmune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility.
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S-EPMC9649734 | biostudies-literature
UnknownIt is time to define an organizational model for the prevention and management of infections along the surgical pathway: a worldwide cross-sectional survey.
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S-EPMC8928018 | biostudies-literature
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